Working at BioPharma Global
Our staff is our competitive edge and we attract the brightest minds in the industry to our consortium of thought leadership.
BIOPHARMA GLOBAL welcomes resume submissions from experienced professionals committed to advancing drug and device development and approval processes internationally.
Our corporate values include innovation, efficiency, collaboration and mutual respect stem from our belief that our work serves others and contributes to a higher purpose in life.
Subject matter expert and staff compensation is paramount – none of the contributions we make as an organization to improving people’s lives could occur without our hardworking professional staff members.
Employee benefits include but are not limited to:
- health insurance for the employee and their family
- generous quantities of personal leave time
- remote work opportunities
- federal and floating holidays
- retirement plan with matching program
- professional continuing education
If being a part of a high performing, respectful team that impacts thousands of lives a year sounds like somewhere you’d like to make a long term commitment to, we would love to hear from you.
Regulatory affairs professionals with US FDA or EU EMA approval process experience, drug and device subject matter experts, market development representatives, research and executive assistants are encouraged to apply here.